Department of Acupuncture, Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
The Key Laboratory of Chinese Internal Medicine of the Ministry of Education, Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, China.
BMJ Open. 2024 Jul 20;14(7):e080743. doi: 10.1136/bmjopen-2023-080743.
Benign prostatic hyperplasia (BPH) is a condition commonly seen among men aged over 40, significantly affecting their quality of life and typically accompanied by lower urinary tract symptoms (LUTS). Acupuncture presents a potentially effective treatment option; however, the exact effects remain uncertain. Therefore, we design this multicentre randomised trial to evaluate the efficacy and safety of electroacupuncture (EA) for relieving LUTS in men with BPH.
A two-arm, sham-controlled, subject-blinded and assessor-blinded trial will be conducted in 11 hospitals in China to compare EA with sham electroacupuncture (SA) in treating moderate to severe LUTS of BPH among men aged 40-80. A total of 306 eligible male patients will be recruited and assigned at a 1:1 ratio to receive either EA or SA for 24 sessions over a succession of 8 weeks, with 24 weeks of follow-up. The primary outcome will be the proportions of participants with at least 30% reduction in the International Prostate Symptom Score total score from baseline at weeks 8 and 20. All statistical analyses will be conducted in accordance with the intention-to-treat principle, and a two-tailed p value less than 0.05 will be considered statistically significant.
The trial has been approved by the institutional review board of Guang'anmen Hospital (2022-203-KY), as well as other recruitment centres. Each participant will receive the detailed information of the trial, and sign the written informed consent. The results of the trial are expected to be published in a peer-reviewed journal.
NCT05585450.
良性前列腺增生(BPH)是一种常见于 40 岁以上男性的疾病,严重影响其生活质量,通常伴有下尿路症状(LUTS)。针灸是一种潜在有效的治疗方法,但确切疗效仍不确定。因此,我们设计了这项多中心随机试验,以评估电针对缓解 BPH 男性 LUTS 的疗效和安全性。
在中国 11 家医院进行的一项两臂、假对照、受试者盲法和评估者盲法试验,将比较电针对(EA)与假电针对(SA)治疗 40-80 岁男性中重度 BPH 的 LUTS。共招募 306 名符合条件的男性患者,按 1:1 比例随机分为 EA 组或 SA 组,分别接受 24 次治疗,持续 8 周,随访 24 周。主要结局是从基线开始的第 8 周和第 20 周,国际前列腺症状评分总评分至少降低 30%的参与者比例。所有统计分析将按照意向治疗原则进行,双尾 p 值小于 0.05 被认为具有统计学意义。
该试验已获得广安门医院(2022-203-KY)以及其他招募中心的机构审查委员会的批准。每位参与者将获得试验的详细信息,并签署书面知情同意书。预计试验结果将发表在同行评议的期刊上。
NCT05585450。